Rate of missed oesophageal cancer at routine endoscopy and survival outcomes: A multicentric cohort study

Abstract

Background

Missed oesophageal cancer (MEC) at upper gastrointestinal endoscopy (UGE) is poorly documented.

Objective

The objectives of this study were: (1) to assess the rate, predictors and survival of MEC; (2) to compare MEC and non-MEC tumours.

Methods

This was a retrospective cohort study conducted at four tertiary centres. Oesophageal cancers (ECs) diagnosed between 2008 and 2015 were included. Patients with a premalignant condition (Barrett, achalasia), prior diagnosis of EC or oesophagogastric junction tumour of gastric origin were excluded. MEC was defined as EC detected within 36 months after negative UGE.

Results

123,395 UGEs were performed during the study period, with 502 ECs being diagnosed (0.4%). A total of 391 ECs were finally included. Overall MEC rate was 6.4% (95% confidence intervals (CI): 4.4–9.3%). The interval between negative and diagnostic UGE was less than 2 years in 84% of the cases. Multivariate analysis showed that a negative endoscopy was associated with proton pump inhibitor (PPI) therapy and less experienced endoscopists. MEC was smaller than non-MEC at diagnosis (25 versus 40 mm, p = 0.021), more often flat or depressed (p = 0.013) and less frequently diagnosed as metastatic disease (p = 0.013). Overall 2-year survival rate was similar for MEC (20%) and non-MEC (24.1%) (p = 0.95).

Conclusions

MEC accounted for 6.4% of all ECs and was associated with poor survival. High-quality UGE and awareness of MEC may help to reduce its incidence.

Keywords

Missed cancer oesophagogastroduodenoscopy oesophageal neoplasms oesophagitis survival

Key summary

Summarize the established knowledge on this subject

Oesophageal cancer is the eighth most common cancer worldwide.

Little is known about oesophageal cancer arising in patients with a recent negative endoscopy.

What are the significant and/or new findings of this study?

Missed oesophageal carcinoma is infrequent in patients without known premalignant conditions, but accounted for 6.4% of all oesophageal cancers.

Survival of patients with missed oesophageal carcinoma is low and not different from non-missed cancer.

Proton pump inhibitor (PPI) therapy and an inexperienced endoscopist are independent predictive factors for missed oesophageal carcinoma.

High-quality endoscopy and adhering to guideline-based recommendations may reduce its incidence.

Introduction

Oesophageal cancer (EC) is the eighth most common cancer worldwide and the sixth leading cause of cancer-specific mortality with an estimated incidence rate of 456,000 per year.¹ Despite improvements in diagnostic techniques and therapy in recent years, the 5-year overall survival of EC remains below 20% in western countries.² Tumour stage at diagnosis is the main prognostic factor in EC patients, and only those with localized disease hold the opportunity to be treated with curative intention. Unfortunately, early symptoms are usually subtle or non-specific, resulting in an unresectable or metastatic disease stage at the time of diagnosis in more than 50% of cases.³ Recent studies suggest that early EC treated with either surgery or endoscopic resection achieves excellent 5-year survival rates (75–90%).^4,5 Therefore, early detection of small lesions and mucosal abnormalities becomes of extreme importance to improve survival.

In the last decade, several studies have questioned the accuracy of endoscopy for early diagnosis of gastrointestinal neoplasms. Interval colorectal cancer has been extensively studied and its prevalence has been estimated to range from 1.8% to 9%.⁶ Studies addressing missed upper gastrointestinal tumours have also found that 4.6% to 25.8% of patients had a negative endoscopy within 3 years before diagnosis.⁷ Nevertheless, the number of studies is limited, and most of them have focused on gastric cancer or adenocarcinoma arising from previously diagnosed Barrett's oesophagus (BE).^7–12 Missed oesophageal cancer (MEC) is a poorly characterized entity in the non-BE population with only a few retrospective studies in this area, mainly from the UK and with data coming from administrative databases.^11,13 Indeed, MEC characteristics, risk factors and prognosis remain to be established.

The aims of this study were to : (1) assess the rate, predictors and survival of MEC; and (2) compare the characteristics of MEC patients with those of non-MEC.

Materials and methods

This was a retrospective cohort, observational and analytical study conducted at four tertiary academic hospitals that provide universal public health care assistance to an area with a population of 1.7 million people. The study protocol adhered to the principles of the Declaration of Helsinki and was approved by the Ethics Committee for clinical research of the Hospital Universitario Ramón y Cajal (3 November 2017). Informed consent for upper gastrointestinal endoscopy (UGE) was obtained in all cases. The Ethics Committee determined that written informed consent was not required in this study due to its retrospective design.

Study population and procedures

All patients who underwent UGE between January 2008 and December 2015 at any of the participating centres were considered for the study, and charts were reviewed. Inclusion criteria for the study were as follows: patients with histology proven EC (adenocarcinoma or squamous cell carcinoma) diagnosed at that period in the participating centres. Exclusion criteria were: (1) prior diagnosis of EC, BE or achalasia; (2) gastroesophageal junction (GEJ) adenocarcinomas of gastric origin; (3) patients with no follow-up at the participating centres; (4) patients referred for treatment from other hospitals with no UGE at any of the participating centres; and (5) more than 10% of the variables with missing values (Figure 1).

Figure 1.

Study flowchart. MEC: missed oesophageal cancer.

Paper (hospital) and electronic (hospital and primary health care) databases of all EC subjects were independently reviewed by two gastroenterologists at each institution. This search included previous negative UGE performed in other public or private hospitals in the same regions. The following demographic and clinical variables were collected: age, sex, tobacco and alcohol consumption as binary categories, EC family history, previous diagnosis of head and neck or lung cancer, obesity (defined as >30 kg/m² body mass index (BMI)), American Society of Anesthesiologists physical status classification (ASA), history of food impaction, UGE indication (dysphagia, haematemesis, melaena and constitutional syndrome were considered alarm symptoms) and medication at both initial negative and final diagnostic endoscopy of MEC.

Gastroscopes used for examination were GIF-Q165, GIF-H180, GIF-H190 (Olympus® Optical, Tokyo, Japan), EG-290KP, EG-294 KP, EG-27I10, EG-29I10, EG-1690K, EG-3490K, EG-2790K (Pentax®, Tokyo, Japan) and EG-530FP, EG-250PES (Fujifilm®, Japan). All procedures were performed or directly supervised by a staff gastroenterologist with expertise in UGE using white light.

Date, sedation (endoscopist propofol-based/endoscopist non-propofol based/anesthesiologist), UGE duration (retrieved as global recording time, i.e. time during which endoscopy software is ready for image or video acquisition), urgent or elective setting, inpatient or outpatient, use of conventional and digital chromoendoscopy (Narrow Band Imaging (NBI), i-scan or Fujinon Intelligent Chromo Endoscopy (FICE) as ascertained by written reports and videos and imaging review), and primary diagnosis were collected from both negative and diagnostic endoscopy records. Size of the lesion, as assessed by the endoscopist (millimetres), presence of ulceration, location (proximal, medial, distal third of oesophagus and GEJ) and tumour morphology (depressed, flat, sessile or mass-like) were obtained from the endoscopy report. We used Siewert–Stein classification for GEJ tumours. Main operators were classified as highly experienced (>5 years as a staff gastroenterologist and >1000 UGEs) or less experienced endoscopist (<5 years and <1000 UGEs).

Histologic subtype (squamous cell carcinoma or adenocarcinoma) and grade of differentiation (undifferentiated–poorly differentiated or moderately well differentiated) were also retrieved from pathology reports.

Tumour stage was determined as per the American Joint Committee on Cancer cTNM system 7th edition.¹⁴ Oncologic treatment was recorded as binary outcomes (Yes/No): neoadjuvant therapy, curative-intent surgery, adjuvant therapy and palliative chemotherapy. Survival status was established using the date of EC diagnosis and the time of death or the date of the last medical visit (in-hospital or primary healthcare) on which the patient was alive.

Study endpoints

The primary outcomes were to assess the proportion and characteristics of MEC. Secondary outcomes were to evaluate the differences between MEC and Non-MEC and between negative UGE and diagnostic UGE in non-MEC. In line with previous research in this field, MEC was defined as EC detected within 36 months after negative UGE.^7,11,13

The presumed reasons for MEC were categorized as: ‘Missed lesion’ (lesion not seen by the endoscopist), ‘Sampling error’ (when a lesion was detected but biopsy sampling was inadequate) and ‘Inappropriate follow-up’ (when a high-risk lesion was present but no proper monitoring was performed).

Statistical analysis

Mean, standard deviation, median and range were calculated for continuous variables and frequency counts and percentages for categorical data. Ninety-five confidence intervals (CI) for proportions were calculated based on the Wilson method. Data were analyzed using parametric methods for normally distributed continuous data (t-test) and non-parametric methods (Mann–Whitney U test) for non-normally distributed continuous data. Chi-squared and Fisher's exact tests were used for categorical data. To decrease the risk of type I error, only those variables previously reported as risk factors for upper gastrointestinal missed cancer or with plausible physiopathological relation with MEC were included in the univariate analysis. All variables included had a rate of missing values less than 5%. Multivariate analysis was performed by using backward stepwise binomial unconditional logistic regression to: (1) detect predictors associated with negative UGE when compared to diagnostic UGE in non-MEC; and (2) identify factors associated with MEC at diagnosis. When more than one negative UGE was available, the most recent UGE was considered for the analysis.

Variables with p values < 0.05 in univariate analysis were included in logistic regression models. The area under the Receiver Operating Characteristic curve was calculated with non-parametric analysis to evaluate the discriminative ability of the logistic models. Goodness-of-fit was assessed using the Hosmer–Lemeshow´ test and pseudo-R² Cragg–Uhler (Nagelkerke).

One-year and 2-year survival probabilities were calculated for MEC and non-MEC using the Kaplan–Meier method and compared with the log-rank test. All analyses were two-tailed, and p values less than 0.05 were considered significant. Analyses were performed at the promoting institution (Hospital Universitario Ramón y Cajal, Madrid) using STATA software version 14.1 (StataCorp. Texas, USA).

Results

During the study period 123,395 UGEs were performed at the four institutions, and 502 ECs were detected (0.41%, 95% CI: 0.37–0.42%). A total number of 391 patients with EC, meeting criteria for the study, were finally included in the analysis (Figure 1). None of the fourteen patients excluded due to no follow-up or missing data had a known previous negative UGE. The majority of the patients were males (87%). Mean age was 66.9 years, standard deviation: 14.7. A total number of 25 MECs were identified (25/123,395 or 1 MEC every 4,936 UGEs). The global rate of MEC was 6.4% (25/391, 95% CI: 4.4–9.3%), without significant differences between centres (6.7%, 6.5%, 6.1%, 6.3%; p = 0.99). The median interval time between negative UGE and MEC diagnosis was 18.6 months (range: 3.2–34.1), and it was below 2 years in 84% of the patients. The median number of negative endoscopies in the MEC group was 1 (range: 1–2). One negative UGE was performed in another hospital. The median duration of all negative UGEs was 5.9 minutes and 5.1 minutes in the subgroup of UGE (n = 15) where no biopsies were taken. The most common finding was oesophagitis (10/25, 40%): three were peptic oesophagitis grade A of Los Angeles Classification, 2 grade B, 2 grade C, 2 grade D and one case of oesophageal candidiasis. Gastritis (9/25, 36%) and peptic-appearing oesophageal stricture (3/25, 12%) were the following most common diagnosis. None of these strictures or peptic oesophagitis were biopsied or properly endoscopically monitored. A detailed analysis of the 25 MECs and the most likely reason for MEC are provided in Table 1. The most common presumed reason for MEC was ‘Missed lesion’ (19/25, 76%), followed by an ‘Inappropriate follow-up’ (6/25, 24%), and ‘Sampling error’ (5/25). One case of MEC (stage II, size: 15 mm) diagnosed after 34 months of the negative UGE was categorized as probable de novo cancer.

Table 1.

Characteristics and reasons for MEC of the 25 cases of oesophageal carcinoma with previous negative endoscopy.

Age (years)	Histologic subtype	Tumour Location (1/3)	Findings at negative UGE	Interval between UGE (months)	Stage and size	Reason for MEC
Interval between UGE: <1 year
51	Squamous	M	Normal	4	II, 20 mm	Missed lesion
83	Squamous	U	Gastritis	6	II, 25 mm	Missed lesion
63	Squamous	U	Normal	3	II, 23 mm	Missed lesion
68	Adenocarcinoma	EGJ	Reflux oesophagitis grade A	9	III, 30 mm	Missed lesion
64	Squamous	M	Gastritis	6	I, 10 mm	Missed lesion
84	Squamous	D	Peptic-like stenosis. Ultrathin gastroscope used	5	III, complete stenosis	Biopsy not taken Sampling error
64	Squamous	D	Reflux oesophagitis grade D Gastritis	11	IV, 30 mm	Inappropriate follow-up Missed lesion
53	Squamous	M	Gastritis	9	III, 35 mm	Missed lesion
66	Squamous	D	Gastric angiodysplasia	5	II, 22 mm	Missed lesion
Interval between UGE: 1–2 years
67	Squamous	M	Nonobstructive peptic-like stenosis at M 1/3 Food bolus impaction	21	III, 25 mm	Biopsy not taken Inappropriate follow-up Sampling error
85	Squamous	U	Nonobstructive peptic-like stenosis at M 1/3 Food bolus impaction Gastritis	13	III, 40 mm	Biopsy not taken Inappropriate follow-up Sampling error
53	Squamous	D	5-mm unspecific oesophageal ulcer at D 1/3 Gastritis	19	II, 20 mm	Biopsy not taken Sampling error
70	Adenocarcinoma	D	Reflux oesophagitis grade D Gastritis	23	III, 25 mm	Inappropriate follow-up Missed lesion
61	Adenocarcinoma	D	Schatzki ring Food bolus impaction	14	IV, 22 mm	Missed lesion Inappropriate follow-up
62	Squamous	M	Gastritis 3-mm oesophageal erosion at M 1/3	20	III, 25 mm	Biopsy not taken Sampling error
78	Adenocarcinoma	D	Reflux oesophagitis grade B	23	III, 20 mm	Missed lesion
67	Squamous	D	Reflux oesophagitis grade B	19	III, 30 mm	Missed lesion
68	Squamous	M	Reflux oesophagitis grade A Food within the stomach	18	II, 18 mm	Missed lesion
64	Adenocarcinoma	D	Normal Poor tolerance of UGE	22	III, 20 mm	Missed lesion
61	Adenocarcinoma	D	Reflux oesophagitis grade A	20	IV, 40 mm	Missed lesion
68	Adenocarcinoma	EGJ	Reflux oesophagitis grade C Gastritis	21	III, 35 mm	Inappropriate follow-up Missed lesion
Interval between UGE: 2–3 years
86	Adenocarcinoma	D	Gastritis	34	II, 15 mm	De novo cancer?
76	Squamous	U	Oesophageal candidiasis	25	IV, 37 mm	Missed lesion No endoscopic reevaluation
79	Adenocarcinoma	D	Reflux oesophagitis grade C	26	IV, 25 mm	Missed lesion
71	Squamous	M	Normal	27	III, 35 mm	Missed lesion

UGE: upper gastrointestinal endoscopy; MEC: missed oesophageal cancer; U: upper; M: middle; D: distal; EGJ: oesophagogastric junction.

Univariate analysis and binomial logistic regression intended to detect predictors of negative UGE in MEC patients are outlined in Table 2. Proton pump inhibitor (PPI) therapy (OR: 10.6, p = 0.021) and endoscopist experience ( < 5 years and < 1000 UGE, OR: 7.41, p = 0.027) were independently associated with a negative UGE.

Table 2.

Comparative analysis: Initial negative endoscopy in MEC patients versus diagnostic endoscopy in non-MEC patients.

	Initial negative endoscopy in MEC patients (n = 25)	Diagnostic endoscopy in non-MEC patients (n = 366)	Univariant (p values)	Binomial logistic regression P-Hosmer-Lemeshow = 0.48 Pseudo-R² Nagelkerke = 0.71, AUC = 0.79
Age, years (median)	66.7	66.8
Male sex	84%	87.1%
PPI therapy	72%	40.3%	0.002	OR = 10.6 (CI 95%: 1.8–75.6), p = 0.021 ^a
Smoking habit	76%	72.4%	0.7
Alcohol	64%	50%	0.16
Family history of EC	19%	12%	0.24
Inpatients	8%	12.6%	0.75
Prior HN or lung tumour	8%	6.7%
Obesity (BMI > 30)	12%	11.5%
Previous food impaction	0%	1%
Food impaction at endoscopy	12%	8.2%	0.46
ASA
I	8%	17.3%
II	32%	43.4%
III	60%	39.1%	0.12
Elective endoscopy	88%	95.8%	0.13
Alarm symptoms	72%	89.6%
Dysphagia	52%	68.9%
Constitutional syndrome	12%	15%
Haematemesis	4%	3.3%
Melaena	4%	2.2%	0.08
Non-alarm symptoms
Pyrosis	36%	24.6%
Dyspepsia	20%	18%
Others	12%	16.8%	0.23
High-definition endoscope	60%	68.3%	0.38
Conventional chromoendoscopy	4%	7.1%	1
Digital chromoendoscopy	4%	5.4%	1
Sedation	20%	33.7%	0.16
No sedation	80%	66.3%
Propofol endoscopist	8%	8%
Non-propofol endoscopist	8%	22.2%
Anaesthesiologist	4%	3.6%	0.31
Endoscopist experience (<5 years)	52%	19.5%	0.001	OR=7.41 (CI 95%: 1.9–55.6), p = 0.027 ^a

Non-MEC: non-missed oesophageal cancer; PPI: proton pump inhibitor; EC: oesophageal cancer; HN: head and neck; BMI: body mass index; ASA: American Society of Anesthesiologist classification; CI: confidence interval.

The second model was estimated to identify factors associated with MEC at diagnosis and it is detailed in Table 3. MEC tumours were smaller than non-MEC (median size: 25 versus 40 mm, OR = 0.97, p = 0.021), more often diagnosed as depressed-flat lesions (28% versus 7.7%, OR = 3.71, p = 0.013) and less likely to be encountered as distant metastatic disease (20% versus 44%, OR = 4.87, p = 0.013).

Table 3.

Comparative analysis: MEC versus non-MEC at diagnosis.

	MEC (n = 25)	Non-MEC (n = 366)	Univariant	Binomial logistic regression P-Hosmer-Lemeshow = 0.51 Pseudo-R² Nagelkerke = 0.66 AUC = 0.80
High-definition endoscope	72%	68.7%	0.39
Food impaction at endoscopy	16%	8.2%	0.25
Alarm symptoms	86%	89.6%
Dyphagia	62%	67.8%
Constitutional syndrome	16%	14.1%
Haematemesis	4%	3.5%
Melaenas	4%	4.2%	0.52
Median tumour size (mm)	25	40	0.0001	OR = 0.97 (CI 95%: 0.94–0.99), p = 0.021
Conventional chromoendoscopy	8%	7.1%	0.69
Digital chromoendoscopy	8%	5.4%	0.64
Tumour location
Proximal oesophagus	16%	10%
Mid oesophagus	28%	31%
Distal oesophagus	48%	45%
GEJ	8%	14%	0.63
Tumour location S*
Proximal oesophagus	25%	15%
Mid oesophagus	44.8%	47%
Distal oesophagus	31.2%	35%
GEJ	0%	3%	0.69
Morphology
Flat-depressed	28%	7.7%
Sessile-mass	72%	92.3%	0.004	OR = 3.71 (CI 95%: 1.31–10.5), p = 0.013
Histology
Squamous cell	64%	61%
Adenocarcinoma	36%	39%	0.9
Grade of differentiation:
Undifferentiated–poorly	38%	46%
Moderately well	62%	54%	0.47
Curative-intent surgery	36%	19%	0.04	p n.s
Palliative chemotherapy	80%	67%	0.17
Cancer stage:
I	4%	3.6%
II	28%	13.5%
III	48%	38.7%
IV	20%	44.3%	0.04
Local (I–III)	80%	56%
Metastatic (IV)	20%	44%	0.02	OR = 4.87 (CI 95%: 1.4–17), p = 0.013

MEC: missed oesophageal cancer; GEJ: gastroesophageal junction; CI: confidence interval; n.s.: non-significant; S: squamous.

*Stratified subanalysis of tumour location for squamous oesophageal cancer.

Survival analysis did not show any significant differences between both groups and it is summarized in Figure 2.

Figure 2.

Survival analysis. MEC: missed oesophageal cancer. 95% Confidence intervals given in parentheses.

Discussion

Results from this multicentric cohort study support that MEC is relatively frequent at routine UGE in tertiary referral centres, with an overall MEC rate as high as 6.4% (CI 95%: 4.4–9.3%) among newly diagnosed EC. Unfortunately, a head-to-head rate comparison with previous reports may not be possible for several reasons (Supplementary Table 1):

MEC definition: remains controversial and is not uniform across studies. The natural history of early EC is poorly understood, but reports from untreated patients indicate that both squamous and adenocarcinomas may take several years to progress from an early to advanced neoplasia.^15,16 Fujita et al. suggested a doubling time of 2–3 years for gastric cancer, and most authors have considered an interval time of from 6 months up to 3.5 years.^{7–9,12,13,15–18} Cancer within the first 3–6 months of a negative UGE has usually been excluded, because information from administrative databases was not precise enough to determine if these UGE were part of the diagnostic work-up.^11,19 Considering that we had access to detailed medical records, we decided to include all cases with a negative UGE within 3 years before EC diagnosis and perform a case-by-case analysis.

Different target population: To our knowledge, this is the first report coming from Southern Europe. Therefore, population lifestyle and healthcare systems may significantly differ from previous reports. These factors may certainly influence cancer epidemiology, diagnosis and outcomes.^20,21

Different selection criteria: Some studies did not exclude patients with GEJ tumours of gastric origin or those with premalignant conditions such as BE or achalasia. These last two subgroups represent a single high-risk population that undergoes specific surveillance protocols and diagnostic techniques. Furthermore, EC in achalasia and BE patients has unique molecular characteristics and natural history that make it a different story.^22,23 As a matter of fact, MEC rate in BE is known to be considerably high despite close monitoring. A recent meta-analysis has estimated that 25.3% of EC in patients with BE are diagnosed within 1 year after the index negative endoscopy.²⁴ Since we aimed to assess MEC at routine UGE, we considered that a separate analysis from these subgroups was justified.

Our study has found that an inexperienced endoscopist and PPI treatment were independently associated with MEC. This last association had been detected in previous investigations and may be explained by the partial mucosal healing of small mucosal lesions in the distal third of the oesophagus by PPI therapy.^25,26 Female gender, younger age, non-gastroenterologist endoscopist and increasing comorbidity have also been postulated to increase the likelihood of interval upper gastrointestinal cancer.^9,10,12 Noticeably, neither our study (20% MEC versus 33% non-MEC, p = 0.16) nor other investigations have proven that sedation is related to MEC, but some data indicate that moderate sedation increases UGE examination quality and patient satisfaction.²⁷ The low proportion of patients undergoing sedation for UGE in our study does not represent our current standard practice, where propofol-based sedation has been adopted in recent years. Whether these negative results may be attributable to inadequate statistical power remains unclear, but it may indeed be a possibility. From our perspective, adequate sedation is essential for high-quality UGE, as it may enhance the detection of small lesions and possibly decrease the MEC rate.

Other physician-related factors that have been proposed to explain missed cancers in UGE are not to biopsy benign-like lesions, the presence of oesophagitis, obtaining an insufficient number of biopsies, pathological errors or follow-up delay.^12,13 This reinforces the idea that every stricture, ulcer or non-specific oesophageal mucosal abnormality should be biopsied and closely monitored.^11,28 When oesophagitis is severe or atypical in appearance, further endoscopic evaluation should be mandatory in the 6–8 weeks after PPI treatment.^29,30 Remarkably, inappropriate follow-up or sampling error was documented in 36% of the patients that eventually developed MEC.

It is worth mentioning that the median duration of negative UGE was only 5.9 minutes, which may have contributed to MEC. Teh et al. found that examination times longer than 7 minutes were more likely to detect early gastric cancer and dysplasia;³¹ indeed, recent quality standard guidelines in UGE support this minimum duration.²⁸

In our study, only one MEC was diagnosed as a stage I disease, 84% of the cases were diagnosed within 2 years from negative endoscopy and alarm symptoms were common in patients at negative UGE. Besides, MECs were more often encountered as flat or depressed (which could have contributed to missing a lesion), follow-up or biopsy policy were often inappropriate and no differences were found in grade of differentiation.^9–13 Altogether leads us to hypothesize that most MECs were actually ‘true MECs’ secondary to an unrecognized lesion rather than new fast-growing ECs.

The proximal oesophagus was previously reported to be associated with MEC^8,11 in probable relation with a less careful evaluation of this segment. On the other hand, we found that more than half of MECs were located at the distal third of the oesophagus or the GEJ junction without significant differences with non-MEC. As all adenocarcinomas were in the distal third/GEJ, we performed a stratified analysis to explore the relationship between squamous subtype and location, without significant findings either (Table 3).

Another relevant finding of our study was that despite MECs being smaller and less often diagnosed at stage IV, 1-year and 2-year survival rates remained discouraging. This fact highlights the importance of early diagnosis and the consequences of missing a malignant lesion.

Our study has some limitations that should be acknowledged.

Fourteen patients (2.7%) were excluded from the analysis due to missing data or no follow-up. Nonetheless, missing data are a rule rather than an exception in biomedical research and it remained within acceptable standards in our analysis.^32,33

We used the time during which endoscopy software was ready for image acquisition as a surrogate marker of mouth to withdrawal time, since this data was not available. Hence, the median real exploration time for negative UGE was less than 5.9 minutes.

Our MEC rate might be slightly underestimated. The lack of a nationwide cancer registry database in our country prevented us from ascertaining whether patients with a negative UGE at our institution have been subsequently diagnosed with EC at other hospitals. Nonetheless, we consider that the relevance of this fact in our estimations is expected to be low, since healthcare is public and universal in Spain, and patients with EC are ordinarily referred to our centres for treatment.

Finally, the study may be underpowered for the detection of a small difference in survival due to limited sample size.

Among other strengths of our study are that it identifies new predictors of MEC, it provides useful information for clinical practice and represents a recent non-administrative database-based cohort that may contribute to focus the attention on a relevant but often forgotten issue. This problem could be underrated considering that MEC is uncommon at UGE (25 cases out of 123,395 UGEs during a 7-year study period). However, this fact is related to a low incidence of EC in our area and current data indicate that UGE missed cancer rate is above that of colorectal interval cancer.⁶ Consequently, research in this field is pertinent and needed.

Future research should focus on what specific measures in UGE may change the current panorama of delay diagnosis. Digital and conventional chromoendoscopy are known to be useful in high-risk groups; nonetheless, they are time-consuming and its application in every single UGE may be unrealistic and likely inefficient. The low use of chromoendoscopy in our study is explained by the small proportion of early neoplasms, the lack of digital chromoendoscopy in some endoscopes and the limited adoption of this technique in our units until recently. Until more data are available, thorough and slow mucosal interrogation of the whole oesophagus, biopsies of any suspicious lesion and bearing in mind that PPI may mask small irregularities are simple and readily available strategies to earlier detection.

In conclusion, MEC represented 6.4% of all ECs. MEC probably arose from unrecognized or misdiagnosed lesions at negative UGE and was associated with physician-related factors. Raising awareness of MEC among endoscopists, adhering to clinical practice guidelines and improvements in UGE quality may help to reduce its incidence and improve prognosis. Further prospective and randomized studies are awaited to identify the most effective strategies to decrease the rate of upper gastrointestinal missed cancer.

Supplemental Material

Supplemental material for Rate of missed oesophageal cancer at routine endoscopy and survival outcomes: A multicentric cohort study

Supplemental material for Rate of missed oesophageal cancer at routine endoscopy and survival outcomes: A multicentric cohort study by Enrique Rodríguez de Santiago, Nerea Hernanz, Héctor Miguel Marcos-Prieto, Miguel Ángel De-Jorge-Turrión, Eva Barreiro-Alonso, Carlos Rodríguez-Escaja, Andrea Jiménez-Jurado, María Sierra-Morales, Isabel Pérez-Valle, Nadja Machado-Volpato, María García-Prada, Laura Núñez-Gómez, Andrés Castaño-García, Ana García García de Paredes, Beatriz Peñas, Enrique Vázquez-Sequeiros and Agustín Albillos in United European Gastroenterology Journal

Footnotes

Acknowledgement

All authors fully approved the final version of the manuscript.

Declaration of conflicting interests

The authors declare that there is no conflict of interest.

Ethics approval

The study was approved by the Ethics Committee for clinical research of the Hospital Universitario Ramœ Cajal (3 November 2017, code: HRYC: 213-17).

Financial support

This study did not receive any grant or financial support.

Informed consent

Informed consent for upper gastrointestinal endoscopy was obtained in all cases. The Ethics Committee determined that written informed consent was not required in this study due to its retrospective design.

References

International Agency for Research on Cancer/WHO. Fact Sheets by Cancer. http://globocan.iarc.fr/Pages/fact_sheets_cancer.aspx (accessed 21 December, 2017).

Cancer.Net. Esophageal Cancer: Statistics. https://www.cancer.net/cancer-types/esophageal-cancer/statistics (25 June, 2012, accessed 21 December, 2017).

Van Rossum

PSN

Mohammad

Vleggaar

et al.

Treatment for unresectable or metastatic oesophageal cancer: current evidence and trends. Nat Rev Gastroenterol Hepatol 2018; 15: 235–249.

Amin RN, Parikh SJ, Gangireddy VGR, et al. Early esophageal cancer specific survival is unaffected by anatomical location of tumor: population-based study. Can J Gastroenterol Hepatol 2016; Article ID 6132640.

Kamel

Lee

Rahouma

et al.

T1N0 oesophageal cancer: patterns of care and outcomes over 25 years. Eur J Cardiothorac Surg 2018; 53: 952–959.

Lee

Huh

. Clinical and biological features of interval colorectal cancer. Clin Endosc 2017; 50: 254–260.

Menon

Trudgill

. How commonly is upper gastrointestinal cancer missed at endoscopy? A meta-analysis. Endosc Int Open 2014; 2: 46–50.

Raftopoulos

Segarajasingam

Burke

et al.

A cohort study of missed and new cancers after esophagogastroduodenoscopy. Am J Gastroenterol 2010; 105: 1292–1297.

Wang

Loftus

Judge

et al.

Rate and predictors of interval esophageal and gastric cancers after esophagogastroduodenoscopy in the United States. Digestion 2016; 94: 176–180.

10.

Cheung

Evans

Lawrence

et al.

OC-013 How often is upper gastrointestinal cancer missed during endoscopy?. Gut 2013; 62: A6.

11.

Chadwick

Groene

Hoare

et al.

A population-based, retrospective, cohort study of esophageal cancer missed at endoscopy. Endoscopy 2014; 46: 553–560.

12.

Cheung

Menon

Hoare

et al.

Factors associated with upper gastrointestinal cancer occurrence after endoscopy that did not diagnose cancer. Dig Dis Sci 2016; 61: 2674–2684.

13.

Yalamarthi

Witherspoon

McCole

et al.

Missed diagnoses in patients with upper gastrointestinal cancers. Endoscopy 2004; 36: 874–879.

14.

Edge

Compton

. The American Joint Committee on Cancer: the 7th edition of the AJCC cancer staging manual and the future of TNM. Ann Surg Oncol 2010; 17: 1471–1474.

15.

Guanrei

Songliang

et al.

Natural history of early esophageal squamous carcinoma and early adenocarcinoma of the gastric cardia in the People's Republic of China. Endoscopy 1988; 20: 95–98.

16.

Wang

Wei

Hao

et al.

Natural progression of early esophageal squamous cell carcinoma. Zhonghua Zhong Liu Za Zhi 2010; 32: 600–602.

17.

Pimenta-Melo

Monteiro-Soares

Libânio

et al.

Missing rate for gastric cancer during upper gastrointestinal endoscopy: a systematic review and meta-analysis. Eur J Gastroenterol Hepatol 2016; 28: 1041–1049.

18.

Fujita

. Biology of early gastric carcinoma. Pathol Res Pract 1978; 163: 297–309.

19.

Hashimoto

Brodt

Skelly

et al.

Administrative database studies: goldmine or goose chase?. Evid Based Spine Care J 2014; 5: 74–76.

20.

Schwingshackl L, Schwedhelm C, Galbete C, et al. Adherence to Mediterranean diet and risk of cancer: an updated systematic review and meta-analysis. Nutrients. Epub ahead of print 25 September 2017. DOI: 10.3390/nu9101063.

21.

Tsai

M-C

Wang

C-C

Lee

H-L

et al.

Health disparities are associated with gastric cancer mortality-to-incidence ratios in 57 countries. World J Gastroenterol 2017; 23: 7881–7887.

22.

Lacerda

Cruvinel-Carloni

de Oliveira

ATT

et al.

Mutational profile of TP53 in esophageal squamous cell carcinoma associated with chagasic megaesophagus. Dis Esophagus 2017; 30: 1–9.

23.

Gibson

Dhaliwal

Clemons

et al.

Barrett's esophagus: cancer and molecular biology. Ann N Y Acad Sci 2013; 1300: 296–314.

24.

Visrodia

Singh

Krishnamoorthi

et al.

Magnitude of missed esophageal adenocarcinoma after Barrett's esophagus diagnosis: a systematic review and meta-analysis. Gastroenterology 2016; 150: 599–607.

25.

Bramble

Suvakovic

Hungin

. Detection of upper gastrointestinal cancer in patients taking antisecretory therapy prior to gastroscopy. Gut 2000; 46: 464–467.

26.

Panter

O'Flanagan

Bramble

et al.

Empirical use of antisecretory drug therapy delays diagnosis of upper gastrointestinal adenocarcinoma but does not affect outcome. Aliment Pharmacol Ther 2004; 19: 981–988.

27.

McQuaid

Laine

. A systematic review and meta-analysis of randomized, controlled trials of moderate sedation for routine endoscopic procedures. Gastrointest Endosc 2008; 67: 910–923.

28.

Sharaf

Shergill

et al. ASGE Standards of Practice Committee . Endoscopic mucosal tissue sampling. Gastrointest Endosc 2013; 78: 216–224.

29.

Beg

Ragunath

Wyman

et al.

Quality standards in upper gastrointestinal endoscopy: a position statement of the British Society of Gastroenterology (BSG) and Association of Upper Gastrointestinal Surgeons of Great Britain and Ireland (AUGIS). Gut 2017; 66: 1886–1899.

30.

Katz

Gerson

Vela

et al.

Guidelines for the diagnosis and management of gastroesophageal reflux disease. Am J Gastroenterol 2013; 108: 308–328.

31.

Teh

Tan

Lau

LJF

et al.

Longer examination time improves detection of gastric cancer during diagnostic upper gastrointestinal endoscopy. Clin Gastroenterol Hepatol 2015; 13: 480–487.

32.

Dong

Peng

C-YJ

. Principled missing data methods for researchers. Springerplus 2013; 2: 222.

33.

Lang

Little

. Principled missing data treatments. Prev Sci 2018; 19: 284–294.

Supplementary Material

Please find the following supplemental material available below.

For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.

For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.

0.00 MB

0.15 MB